FDA Label for Desonide

View Indications, Usage & Precautions

Desonide Product Label

The following document was submitted to the FDA by the labeler of this product Aleor Dermaceuticals Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Package Label.Principal Display Panel



TUBE LABEL

Rx Only

NDC 71589-005-15

Desonide Ointment, 0.05%

FOR EXTERNAL USE ONLY

NOT FOR OPHTHALMIC USE

NET WT 15 grams

CARTON LABEL

Rx Only

NDC 71589-005-15

Desonide Ointment, 0.05%

FOR EXTERNAL USE ONLY

NOT FOR OPHTHALMIC USE

NET WT 15 grams


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